-
Notifications
You must be signed in to change notification settings - Fork 63
Change log
nwillhoft edited this page Oct 17, 2024
·
71 revisions
Please note all dates are expressed as ISO-8601.
-
[/ga4gh/beacon/query]
Update output format -
[overlap/translation/:id]
Use protein feature description if no InterPro xref exists -
[/vep]
Add VEP plugins REVEL and ClinPred -
[/vep]
Add LOEUF plugin to VEP REST -
[/vep]
Update dbNSFP data to 4.7c -
[/vep/]
and[variation/]
endpoints have additional gencode_primary flag
-
"GET regulatory/species/:species/id/:id:"
removed -
"GET regulatory/species/:species/epigenome:"
removed -
"GET regulatory/species/:species/microarray/:microarray/vendor/:vendor:"
removed -
"GET regulatory/species/:species/microarray:"
removed -
"GET regulatory/species/:species/microarray/:microarray/probe/:probe:
" removed -
"GET regulatory/species/:species/microarray/:microarray/probe_set/:probe_set:"
removed -
"GET overlap/region/:species/:region:"
updated (other_regulatory and array_probe removed as possible feature types) -
"GET overlap/id/:id:"
update (other_regulatory and array_probe removed as possible feature types)
-
[/variation/:species/id]
Return structural variants by their ID -
[/variation/:species]
Return structural variants by their ID -
[/vep/:species/id]
Return structural variants by their ID -
[/vep/:species]
Return structural variants by their ID -
[/vep/:species/hgvs/]
New plugin option added: DosageSensitivity -
[/vep/:species/id/]
New plugin option added: DosageSensitivity -
[/vep/:species/region/]
New plugin option added: DosageSensitivity -
[/vep]
Added AlphaMissense plugin -
[/vep]
Update README URL for dbNSFP 4.5c -
[/vep/:species/hgvs/]
New option values allowed for: CADD -
[/vep/:species/id/]
New option values allowed for: CADD -
[/vep/:species/region/]
New option values allowed for: CADD
"GET cafe/genetree/member/id/:id"
"GET genetree/member/id/:id"
"GET homology/id/:id"
-
[/cafe/genetree/member/id/:id]
is deprecated and replaced by[/cafe/genetree/member/id/:species/:id]
-
[/genetree/member/id/:id]
is deprecated and replaced by[/genetree/member/id/:species/:id]
-
[/homology/id/:id]
is deprecated and replaced by[/homology/id/:species/:id]
-
[/vep]
Documented OpenTargets plugin -
[/vep]
Documented MaveDB plugin -
[/vep]
Documented Enformer plugin -
[/ga4gh/beacon/query]
Return VEP data in Beacon output -
[/lookup/]
Added length attribute for transcript feature
-
[/vep]
Documented MaveDB plugin -
[/vep]
MentionALL
keyword in documentation of dbNSFP plugin for VEP -
[/vep]
Added Geno2MP plugin -
[/vep]
Documented use of transcript_match option for dbNSFP plugin -
[/ga4gh/beacon]
Upgraded Beacon to version 2 -
[/ga4gh/beacon/query]
Implement the Beacon response following specifications for version 2 -
[/vep]
Documented all valid flags in VEP REST -
[/variant_recoder]
Documented all valid flags in VR REST -
[/vep]
Allow to output the GA4GH Variation Representation Specification (VRS) standard -
[/variant_recoder
] Allow to output the GA4GH Variation Representation Specification (VRS) standard
-
[/vep/:species/hgvs/]
new plugin option added: UTRAnnotator -
[/vep/:species/id/]
new plugin option added: UTRAnnotator -
[/vep/:species/region/]
new plugin option added: UTRAnnotator
-
[/ga4gh/beacon]
Added the dataset dbSNP -
[/ga4gh/beacon/query]
Fix bug: the response includes the dataset dbSNP if the query includes the dataset response -
[/vep/:species/hgvs/]
new plugin option added: NMD -
[/vep/:species/id/]
new plugin option added: NMD -
[/vep/:species/region/]
new plugin option added: NMD
-
[/overlap]
and[/overlap/region]
Removed all references to peak type value for the Feature parameter -
[/vep/:species/hgvs/]
New plugin option added: mutfunc. Plugin option removed: SpliceRegion -
[/vep/:species/id/]
New plugin option added: mutfunc. Plugin option removed: SpliceRegion -
[/vep/:species/region/]
New plugin option added: mutfunc. Plugin option removed: SpliceRegion -
[/family]
Deprecated and removed the gene family endpoint
-
[/vep/:species/hgvs/]
New plugin options added: IntAct, EVE, and GO. Plugin option available: AncestralAllele -
[/vep/:species/id/]
New plugin options added: IntAct, EVE, and GO. Plugin option available: AncestralAllele -
[/vep/:species/region/]
New plugin options added: IntAct, EVE, and GO. Plugin option available: AncestralAllele
-
[vep/:species/hgvs/:hgvs_notation]
New plugin option added to select SpliceAI annotation scores from Ensembl MANE transcripts (SNV only) -
[vep/:species/id/:id]
New plugin option added to select SpliceAI annotation scores from Ensembl MANE transcripts (SNV only) -
[vep/:species/region/:region/:allele/]
New plugin option added to select SpliceAI annotation scores from Ensembl MANE transcripts (SNV only)
-
[variant_recoder/:species/:id]
Has the option to return VCF and variation synonyms -
[/lookup]
and[/overlap]
Added the canonical_transcript attribute to gene object, to provide the stable ID of the canonical transcript for that gene -
[/lookup]
Added MANE object. Available only with the expand=1 and mane=1 option -
[/overlap]
Added MANE object. Available with the feature=mane option -
[eqtl/]
eQTL endpoints have been removed and replaced by the new eQTL catalogue API at https://www.ebi.ac.uk/eqtl/
-
[/overlap]
Added is_canonical attribute for transcript feature, for consistency with the lookup endpoint -
[/lookup]
Added version attribute for translation feature in full format (already available in condensed format)
-
[info/assembly/:species]
"base_pairs" removed from response. Use "golden_path" instead. -
[/vep/:species/hgvs/]
SpliceAI and DisGeNET options return data in key-value pair structures rather than concatenated strings of results -
[/vep/:species/id/]
SpliceAI and DisGeNET options return data in key-value pair structures rather than concatenated strings of results -
[/vep/:species/region/]
SpliceAI and DisGeNET options return data in key-value pair structures rather than concatenated strings of results
-
[/vep/:species/hgvs/]
new plugin option added: Mastermind -
[/vep/:species/id/]
new plugin option added: Mastermind -
[/vep/:species/region/]
new plugin option added: Mastermind -
[variant_recorder/:species/:id]
Identifiers are now reported separately for each alternative allele of the input variant
-
[/vep/:species/hgvs/]
new plugin option added: DisGeNet -
[/vep/:species/id/]
new plugin option added: DisGeNet -
[/vep/:species/region/]
new plugin option added: DisGeNet
-
[/vep/*]
VEP endpoints updated to contain transcription_factors key for motif_feature_consequences -
[/phenotype/gene/:species/:gene]
New options added: trait, tumour, non_specified -
[/phenotype/region/:species/:gene]
New options added: trait, tumour, non_specified -
[/alignment/region/:species/:region]
Method 'EPO_LOW_COVERAGE' replaced by 'EPO_EXTENDED'
-
[variation/:species/:id]
: The ancestral_allele field is now reported in each location hash of the mappings array -
[/vep]
: Added the flags--shift_3prime
and--shift_genomic
to allow for the 3' shifting of insertions and deletions in repetitive regions before consequence calculation -
[/vep/:species/hgvs/]
New plugin option added: SpliceAI -
[/vep/:species/id/]
New plugin option added: SpliceAI -
[/vep/:species/region/]
New plugin option added: SpliceAI
-
[/info/variation/consequence_types]
: Added option to include the consequence ranking for the sequence ontology terms
-
[/vep/:species/hgvs/]
: new options: CADD, mane, vcf_string, transcript_version, SpliceRegion, LoF -
[/vep/:species/id/]
: new options: CADD, mane, vcf_string, transcript_version, SpliceRegion, LoF -
[/vep/:species/region/]
: new options: CADD, mane, vcf_string, transcript_version, SpliceRegion, LoF
-
[/ld/:species/region]
: corrected maximum region size in documentation
-
[/ga4gh/beacon/query]
: Add support to structural variants with new fields variantType and start (optional in case of sv); changed message error display
-
[/variant_recorder]
documentation updates
-
[regulatory/species/:species/epigenome]
will return the following fields:[description, short_name, efo_accession, encode_accession, epirr_accession, full_name, name, search_terms]
-
[info]
endpoints now available for vertebrate species
-
[variant_recoder/]
Also retrieve a SPDI for a given variant identifier, HGVS or SPDI notation. -
[species/:species/binding_matrix/:binding_matrix_stable_id/]
'max_element' key has been replaced by 'max_position_sum' in order to fix a scaling issue of the binding matrix widget -
[overlap/id/:id]
and[overlap/region/:species/:region]
Motif features will now contain a list of all the associated Transcription Factor complexes -
comparative genomics
endpoints accept any compara database across all divisions (vertebrates, plants, fungi, metazoa, protists, bacteria, pan_homology)
-
[alignment/region]
returns undef when none of the display species is found - Add missing translation end for variants
-
[/stats]
Display basic server statistics
-
[/variation/:species/:id?pops=1]
for population allele frequencies with no allele count, the allele_count property is not returned instead of incorrectly returning 0 -
[/vep/:species]
remove documentation of CSN option due to relevant plug-in having been removed
- cpanfile now includes Perl modules required to correctly render all error messages
- fixed broken URL pointing to the Ensembl Variation documentation
- the server now creates log and PID directories during start-up if they don't exist, and checks if their respective permissions are sane
- Support for gnomAD data in Variation endpoints
- Reconciling of allele frequencies from VEP endpoints to match downloadable VEP tool. This is a breaking change, of the abbreviation "maf" being replaced with "af"
- Phenotype endpoints now report ontology terms of phenotypes
- Fix in gene tree and alignment endpoints to no longer report a zero on the root nodes
- Enrichment of family endpoint has changed the output format
- New genotyping_chips option in variation endpoint
- New endpoints
[biotypes/name]
,[biotypes/groups]
. These can be used for example to find all coding biotypes, or to learn more about a particular biotype - New endpoint
[/species/:species/binding_matrix/:binding_matrix_stable_id]
to retrieve binding matrices of a species -
[info/variation/population]
REST endpoint to allow retrieval of individual names and any genders for a given population - Phenotype endpoints now return MIM ids if possible, optionally Pubmed IDs, review status and submitter names
- Produce an error if a user tries to request a cds or protein type in the sequence endpoint using an exon id
-
[/info/biotypes/groups]
endpoint to retrieve list of available biotype groups -
[/info/biotypes/groups/:group/:object_type]
endpoint to retrieve the properties of biotypes within provided group (and object_type) -
[/info/biotypes/name/:name/:object_type]
endpoint to retrieve the properties of biotypes with provided name (and object_type)
-
[/vep/:species/*]
Created a frequency entry in the colocated variants entry and removed all *_maf and *_allele entries which previously reported allele frequencies. Allele frequencies are now stored in the frequency entry for a colocated variant. Allele frequencies are now reported for each alternative allele of the input variant. Allele frequencies if available are reported for the following populations: 1000 Genomes Project: afr, amr, asn, eas, eur, sas; ESP: aa, ea; gnomAD: gnomad_afr, gnomad_amr, gnomad_asj, gnomad_eas, gnomad_fin, gnomad_nfe, gnomad_oth, gnomad_sas -
[/variation]
added genotyping_chips option to the variation endpoint -
[/family]
the output of the family endpoint changed
-
[/phenotype/gene/:species/:gene]
New endpoint to return phenotype annotations for a given gene - Added ambiguity flag to VEP endpoints
-
[/overlap/id]
Removed feature type chipseq and added peak and other_regulatory as allowed feature types - Endpoint examples in R now added
-
[/variant_recorder]
Retrieve all known IDs for a given variant identifier or HGVS notation -
[/variation/pmid]
and[/variation/pmcid]
Retrieve variants by publication
-
[/assembly/*]
Include information about region synonyms -
[/sequence]
Include initial input in output
-
[ga4gh/beacon/*]
New Global Alliance beacon implementation -
[info/variation/consequence_types]
New info endpoint to report all variant consequence types in use by variation endpoints
-
[phenotype/*]
Phenotype descriptions now emitted in alphabetical order. Also seen in[variation/:species]
-
[variation/:species/:id]
Variation endpoint now optionally returning ontology accessions
-
[overlap/*]
Stop returning errors when there is no variation data for a given request with a variation feature type - Updated default server properties for new installations
-
GTEx
data updated to v6 -
[/cafe/genetree]
endpoints, to retrieve information about cafe trees -
[/family]
endpoints, to retrieve information about gene families -
[/phenotype]
endpoints, to retrieve phenotype associations overlapping a defined region -
[/regulatory/species/:species/epigenome]
endpoint which returns information about all epigenomes available for a given species -
[/regulatory/species/:species/microarray]
endpoint to retrieve information about all microarrays available for a given species -
[/regulatory/species/:species/microarray/:microarray]
endpoints for more information on specific microarrays and probes within the microarray
-
[/ga4gh]/
endpoints updated to latest version - Enable more flags in
[/vep]
endpoints - New
attrib
parameter for[/ld]
endpoints, returns more information about the variation -
population_name
is now a required parameter for the[/ld]
endpoints - Changed
[/regulatory/species/:species/:id]
to[/regulatory/species/:species/id/:id]
- Proper handling of
user parameters in POST body
-
include_original_region
option added to[/map]
endpoints - Strain information added to
[/info/species]
endpoint, includinghide_strain_info
andstrain_collection
options - The new 18-murinae whole-genome Cactus alignment can be retrieved with the
/alignment
endpoint -
phenotypes
option added to[/lookup]
endpoints - New
[/phenotype]
endpoints providing phenotype annotation for genomic features - A new version of the
[/VEP]
tool
- VEP dbNSFP data updated to 3.2a
- New VEP endpoint supporting POST vep/:species/hgvs
- New eQTL endpoint providing GTEx V6 gene/cis-variant correlations in 44 human tissues. Searchable by both gene and variant.
- GA4GH endpoints updated to alpha version v0.6.0a4
- VEP endpoints now have additional RefSeq and "merged" caches available
- Reduced search space in Linkage Disequilibrium (LD) endpoint, to maintain quality of service
- LD endpoint returns additional data
- Performance improvements to Compara endpoints
- New Regulation endpoint
[/ld/:species/region/]
to compute LD values between all pairs of variants in a defined region - New variation endpoint
[/transcript_haplotypes]
to compute observed transcript haplotype sequences based on phased genotype data -
[/info/external_dbs/]
now allows restricting the list of external database entries to a specified species - GA4GH endpoints updated to version 0.6.0
-
[/sequence/id]
endpoint now allows start and end parameters allowing trimming of returned sequence - New Information endpoint
[info/variation/populations]
list of populations for a given species
-
[/lookup]
now includes version for stable ids - UTR features can be retrieved from the
[/lookup]
endpoint when using the expand option -
[/overlap]
endpoint now includes gene_id, transcript_id, protein_id, exon_id, havana_gene, havana_transcript and havana_version where available -
[/overlap]
endpoint can now retrieve band information - is_circular attribute added to the
[/info/assembly]
endpoint - minor_allele attribute added to the
[/variation]
endpoint
- the
[/overlap]
endpoint does not include failed variants
-
[/vep]
now includes new attribute "phenotype_or_disease" -
[/variation]
endpoint now has access to additional genotype data for 1000 Genomes phase 3, as well as NextGen cow.
-
[/vep]
[/variation]
endpoints now return populated fields only. No empty elements. -
[/ga4gh]
fix for paging of results.
- Global Alliance endpoints merged onto the same server as Ensembl endpoints. These will no longer be hosted separately.
- POST support for
[/variation]
endpoint - More efficient
[/overlap]
endpoint
-
[/vep]
endpoint properly prioritises user parameters over defaults
- POST support added for
[/sequence]
endpoints - New VEP endpoint
[/hgvs]
to retrieve consequence data based on a HGVS notation -
population_genotype
option added to[/variation]
endpoint -
failed_variation
field added to[/variation]
endpoints -
segmentation
,motif
,chipseq
,array_probe
andfeature_type
options added to[/overlap]
endpoint -
Accept
supported for POST endpoints, to specify the output format of your choice -
orthoXML
format added for[/homology]
endpoints -
coordinate_system
field changed tocoord_system
in[/info/assembly_info]
endpoint
- New Regulatory endpoint
[/regulatory]
to retrieve data from the regulatory build - POST support added for
[/lookup]
endpoints -
is_canonical
for Transcripts andlength
for Translations fields added to[/lookup]
endpoints -
taxon_id
field added to[/homology]
endpoints -
Parent
field added to[/overlap/translation]
endpoints to retrieve corresponding Transcript -
version
for stable_id field added to[/overlap]
endpoints
- An
assembly_name
field has been added to most endpoints, including[/vep]
,[/lookup]
,[/map]
,[/variation]
- Add line break for sequences
- Better error handling in plain type
-
[/vep]
output has been changed to be more json compliant and hierarchic
A transition from beta to a more stable interface for users, better documentation and more functionality. More features will appear over time, but these will not interfere with the existing interface wherever possible.
- New POST endpoints. POST messages allow the user to potentially submit huge quantities of requests, so please be kind, observe any rate and message size limits, and make your clients tolerant to timeouts and errors.
-
[/vep/:species/id/]
,[/vep/:species/region/]
. The VEP endpoints have had their URLs altered, and the existing ID and region endpoints now accept POST messages containing many variants. Regions can be submitted in the formats supported by the VEP (vcf, hgvs, pileup, ensembl, and vep). -
[/archive/id/]
. The archive endpoint now supports lists of IDs in POST messages.
-
-
[/variation]
endpoint that retrieves variants linked to a gene or transcript -
[/genetree/*]
endpoints support JSON response format -
[/feature/*]
endpoints renamed to[/overlap/]
to more closely represent their function -
[/overlap/*]
endpoints now support BED response format -
[/sequence/*]
endpoints now report sequence with contextual soft-masking for features through themask_feature
option. This allows the finding of feature boundaries in raw sequence. IDs of typecds
mask the UTRs, and IDs of typegene
mask introns. - HTTPS support for clients working within a secure environment
- The rate limiter is set to 15 requests per second (an increase from 3)
- Spelling of
[/ontology/descendents]
changed to[/ontology/descendants]
- Documentation overhaul to better explain endpoints and parameters
- Regulatory features appear correctly from
[/overlap/*]
endpoints - Numerous tweaks to error handling and documentation
-
[/assembly/info]
renamed to[/info/assembly]
to match convention
- MessagePack and Sereal formats were receiving little use and have been retired to decrease maintenance burden
-
[/genetree/*]
endpoints no longer supporting phyloxml_aligned and phyloxml_sequence parameters. These have been replaced with aligned and sequence. -
[/location]
endpoints have been replaced by[/overlap]
- New versions of Moose, Catalyst and Catalyst::Action::REST are causing misbehaviour with the server. Please observe the library versions required in the installation makefile until we find a way to fix this conflict.
-
[/feature/]
Trim features from output which overlap 5' or 3' optionally -
[/alignment/region/]
replaces[/alignment/block/region/]
and[/alignment/slice/region/]
- The example for multiple alignments is wrong
- XS assert_ref fails with REST feature endpoint
-
[/feature]
BED output is very slow for transcripts -
[/feature]
BED output; thick and thin ends are incorrect for reverse strand transcripts
- Removed deprecated methods from Compara
- Build a better rate limiter
- Enable compression on REST site
- Ensure rate limiter reports the time scale over which rate limiting occurs
- Faster GeneTree serlialisation; JSON now supported
- Rate limiter responds with a
Retry-After
header once limits have been hit -
[/info/species]
to report common names of species and taxon ids -
[/lookup/:species/:symbol]
Look up the location of an object based on a symbol -
[/taxonomy/name]
Allow for searching of Taxonomy nodes by any linked name
- Detect content in REST does not understand Accepts
- GFF3 for cds features invalid, duplicate ids for simple features
- Serialisations choose to send the
content-type
back astext/plain
-
[/homology]
throws an exception when you ask for orthologues of the species the gene is from -
[/xrefs/symbol/:species/:symbol]
does not respond to object type filtering -
[/xrefs]
fails to report linkage types for GO xrefs
-
[/xrefs]
fails to report linkage types for ontology xrefs -
[/homology/id]
and[/homology/symbol]
failed when querying for the same species as the member
-
[/lookup/id]
and[/xrefs/symbol]
were using the parameter object rather than object_type -
[/homology]
endpoints would accept only one instance of target_taxon and target_species. We now allow multiples as intended
-
[/feature/id]
Querying for features using a negative stranded feature reversed the strand of the retrieved object
- Lookup with a non-indexed stable identifiers in databases other than core failed
- Improved error page when a user goes to an unknown documentation page
- Rate limiter responds with a
Retry-After
header once limits have been hit -
[/assembly/info]
should return those Slices which are part of the karyotype -
[/feature/translation/:id]
Support the retrieval of splice sites with respect from a translation -
[/feature/translation]
Improved translation feature support for GFF3 -
[/info/analysis]
Support retrieval of analysis logic names -
[/info/analysis]
to provide logic names available -
[/info/biotype]
Support for listing available biotypes -
[/info/data]
has been sped up for Ensembl Genomes servers (Ensembl Bacteria) -
[/info/external_db]
Support retrieval of external dbs -
[/info/external_dbs]
Support the retrieval of external dbs -
[/lookup/id]
Provide more information for a lookup ID -
[/info/biotypes]
Support retrieval of biotypes from the rest api
- REST GFF CDS Line is incorrect. ID can repeat in a single GFF file
-
[/compara/homology]
throws an exception when requesting ENSEMBL_PROJECTION ortholog alignmnets -
[/feature/id]
does not work for regulatory regions -
[/feature/id]
is failing as it thinks species is a HASH ref -
[/genetree/symbol]
and[/feature/translation]
modified to default object type -
[/ontology/descendents/:id]
Using the zero_distance parameter destroys any output -
[/ontology/id/:id]
Giving a bogus ontology ID causes a stack trace
-
[/info/species]
allows you to specify a division to limit the data by
-
[/homology/id]
and[/homology/symbol]
have improved error reporting when IDs and symbols cannot be found
##Bugfixes:
-
[/vep]
could not find a region due to changes in the backing Lookup object
-
[/feature/id]
allows for the querying of features overlapping a stable ID -
[/genetree/member/id]
allows for the querying of a GeneTree by one of its member's stable ID -
[/genetree/member/symbol]
allows for the querying of a GeneTree by one of its member's symbols (its name e.g. BRAF) -
[/taxonomy/]
provides methods for querying the Ensembl taxonomy database. This is a mirror of NCBI's taxonomy. -
[/ontology/]
provides methods for querying the Ensembl ontology database -
[/lookup/id]
replaces[/lookup]
but the old endpoint remains active. This endpoint now supports genomic location reporting of features when output format is set to full. Please use the new endpoint. -
Model::Registry
supports use of Ensembl Genomes'Bio::EnsEMBL::LookUp
object to help loading bacteria datasets - All location based services no longer support underscores as a numeric separator. All now support UCSC names for sequence regions
- Support for CrossOrigin resource sharing via
Plack::Middleware::CrossOrigin
-
[/species/info]
now supports the vast numbers Ensembl Bacteria brings into the registry - All models if they need access to the Catalyst context object implement methods to access this without explicit pass throughs. Affects all Models apart from Registry
- Model::Registry has
Bio::EnsEMBL::LookUp
configuration attributes -
Controller::Taxonomy
allows for database name configuration -
Controller::Ontology
allows for database name configuration
- Support for Sereal encoding format from Sereal::Encoder. MIME type
application/x-sereal
is required and extension support is.sereal
- Support for MessagePack encoding format from Data::MessagePack. MIME type
application/x-msgpack
is required and extension support is.msgpack
- Configuration has switched to a more Catalyst friendly method. Config is namespaced to the object which uses it and is accessible via local accessors in that object.
- Registry and Documentation are prefixed with
Model::
- Feature and Sequence are prefixed with
Controller::
- All other configuration sections are unaffected
- Registry and Documentation are prefixed with
-
[/feature]
CDS no longer report a protein as an exon's ID since ID should be unique in a file. Instead this is available via the protein_id attribute
-
[/homology]
now supports the retrieval of CDNA sequences
-
[/feature]
had incorrect documentation WRT features available
-
[/sequence/region]
had not been recoded for our multiple sequence changes resulting in a broken service - Documentation needs to internally escape characters like + for example as Catalyst does not like this
-
[/vep]
was attempting to multipleintron_number
andexon_number
to avoid stringification of numerics; these two fields are not numeric
-
[/feature]
new endpoint for retrieval of features by a genomic location -
[/sequence]
now responds to Content-typetext/plain
with an unformatted raw String of sequence -
Plack::Middleware::Throttle
is an optional install; custom extensions available with this checkout. Brings rate limiting to the REST API service - Using CHI to cache documentation API responses
- Content type detection carried out using file name extensions as well as the existing mechanisms. Supported on all endpoints
-
[/sequence]
supports multiple sequences from a single identifier e.g. proteins from a gene identifier - Online change log
-
[/genetree]
now supports CDNA sequence in PhyloXML output
-
[/vep]
alleles now an array with allele_string explicit instead of as key. -
[/info/species]
reports the division of a species; Ensembl Genomes extension - Mime types changed for many services to denote non-standard types. We now use
text/x-fasta
,text-x-gff3
,text/x-seqxml+xml
andtext/x-phyloxml+xml
. -
[/genetree]
has had NHX format retired in favor of PhyloXML -
[/map]
Translate coordinates for transcript/translation to genomic now reports the sequence region name
- 2 Y regions returned from
[/assembly/info/human]
fixed - JSON serialiser mis-encodes numerics as Strings due to MySQL DBD issues
- Location parser method does not handle
GL1923.1
properly -
[/genetree]
parameter nh_format has no effect on the newick output
- Removal of
<Compara>
configuration option; new code introduced to select the best compara available based upon species.division - Documentation supports variable replacement for easier configuration by third parties
- CHI cache support in configuration; see CHI's POD and our production configuration about how you can configure it
- URL, name and logo now configurable
- Initial revision of REST API
- Support for comparative genomics, cross references, ID lookup, mapping coordinates, sequences & variations
- Information endpoints also made available
- Documentation added for all end points